CNTNAP1

CNTNAP1
Identifiers
Aliases	CNTNAP1, CASPR, CNTNAP, NRXN4, P190, contactin associated protein 1
External IDs	MGI: 1858201 HomoloGene: 2693 GeneCards: CNTNAP1
Gene ontology Molecular function • SH3 domain binding • protein binding • SH3/SH2 adaptor activity • receptor activity Cellular component • integral component of membrane • membrane • myelin sheath • voltage-gated potassium channel complex • integral component of plasma membrane • axon • paranode region of axon Biological process • neuron projection morphogenesis • neuromuscular process controlling posture • neuromuscular process controlling balance • protein localization to paranode region of axon • cell adhesion • cytoskeleton organization • neuronal action potential propagation • paranodal junction assembly • neuron projection development • signal transduction • positive regulation of signal transduction Sources:Amigo / QuickGO
Orthologs
Species	Human	Mouse
Entrez	8506	53321
Ensembl	ENSG00000108797	ENSMUSG00000017167
UniProt	P78357	O54991
RefSeq (mRNA)	NM_003632	NM_016782
RefSeq (protein)	NP_003623.1	NP_058062.2
Location (UCSC)	Chr 17: 42.68 – 42.7 Mb	Chr 11: 101.17 – 101.19 Mb
PubMed search	[1]	[2]
Wikidata

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Contactin associated protein 1 is a protein that in humans is encoded by the CNTNAP1 gene.^[3]

Function

The gene product was initially identified as a 190-kD protein associated with the contactin-PTPRZ1 complex. The 1,384-amino acid protein, also designated p190 or CASPR for 'contactin-associated protein,' includes an extracellular domain with several putative protein-protein interaction domains, a putative transmembrane domain, and a 74-amino acid cytoplasmic domain. Northern blot analysis showed that the gene is transcribed predominantly in brain as a transcript of 6.2 kb, with weak expression in several other tissues tested. The architecture of its extracellular domain is similar to that of neurexins, and this protein may be the signaling subunit of contactin, enabling recruitment and activation of intracellular signaling pathways in neurons. [provided by RefSeq, Jan 2009].

Mutations in CNTNAP1 cause arthrogryposis multiplex congenita .^[4]

References

1. "Human PubMed Reference:".
2. "Mouse PubMed Reference:".
3. "Entrez Gene: Contactin associated protein 1".
4. Laquérriere A, Maluenda J, Camus A, Fontenas L, Dieterich K, Nolent F, et al. (May 2014). "Mutations in CNTNAP1 and ADCY6 are responsible for severe arthrogryposis multiplex congenita with axoglial defects". Human Molecular Genetics. 23 (9): 2279–89. doi:10.1093/hmg/ddt618. PMID 24319099.

Further reading

• Martins-de-Souza D, Guest PC, Mann DM, Roeber S, Rahmoune H, Bauder C, Kretzschmar H, Volk B, Baborie A, Bahn S (April 2012). "Proteomic analysis identifies dysfunction in cellular transport, energy, and protein metabolism in different brain regions of atypical frontotemporal lobar degeneration". Journal of Proteome Research. 11 (4): 2533–43. doi:10.1021/pr2012279. PMID 22360420.
• Velez Edwards DR, Naj AC, Monda K, North KE, Neuhouser M, Magvanjav O, Kusimo I, Vitolins MZ, Manson JE, O'Sullivan MJ, Rampersaud E, Edwards TL (March 2013). "Gene-environment interactions and obesity traits among postmenopausal African-American and Hispanic women in the Women's Health Initiative SHARe Study". Human Genetics. 132 (3): 323–36. doi:10.1007/s00439-012-1246-3. PMC 3704217. PMID 23192594.
• Li R, Zhang B, Zheng Y (December 1997). "Structural determinants required for the interaction between Rho GTPase and the GTPase-activating domain of p190". The Journal of Biological Chemistry. 272 (52): 32830–5. doi:10.1074/jbc.272.52.32830. PMID 9407060.
• Lee JY, Park AK, Lee KM, Park SK, Han S, Han W, Noh DY, Yoo KY, Kim H, Chanock SJ, Rothman N, Kang D (September 2009). "Candidate gene approach evaluates association between innate immunity genes and breast cancer risk in Korean women". Carcinogenesis. 30 (9): 1528–31. doi:10.1093/carcin/bgp084. PMID 19372141.
• Peles E, Nativ M, Lustig M, Grumet M, Schilling J, Martinez R, Plowman GD, Schlessinger J (March 1997). "Identification of a novel contactin-associated transmembrane receptor with multiple domains implicated in protein-protein interactions". The EMBO Journal. 16 (5): 978–88. doi:10.1093/emboj/16.5.978. PMC 1169698. PMID 9118959.
• Hur JY, Teranishi Y, Kihara T, Yamamoto NG, Inoue M, Hosia W, Hashimoto M, Winblad B, Frykman S, Tjernberg LO (April 2012). "Identification of novel γ-secretase-associated proteins in detergent-resistant membranes from brain". The Journal of Biological Chemistry. 287 (15): 11991–2005. doi:10.1074/jbc.M111.246074. PMC 3320946. PMID 22315232.
• Venken K, Meuleman J, Irobi J, Ceuterick C, Martini R, De Jonghe P, Timmerman V (August 2001). "Caspr1/Paranodin/Neurexin IV is most likely not a common disease-causing gene for inherited peripheral neuropathies". Neuroreport. 12 (11): 2609–14. doi:10.1097/00001756-200108080-00063. PMID 11496158.
• Charles P, Tait S, Faivre-Sarrailh C, Barbin G, Gunn-Moore F, Denisenko-Nehrbass N, Guennoc AM, Girault JA, Brophy PJ, Lubetzki C (February 2002). "Neurofascin is a glial receptor for the paranodin/Caspr-contactin axonal complex at the axoglial junction". Current Biology. 12 (3): 217–20. doi:10.1016/S0960-9822(01)00680-7. PMID 11839274.
• Nie DY, Zhou ZH, Ang BT, Teng FY, Xu G, Xiang T, Wang CY, Zeng L, Takeda Y, Xu TL, Ng YK, Faivre-Sarrailh C, Popko B, Ling EA, Schachner M, Watanabe K, Pallen CJ, Tang BL, Xiao ZC (November 2003). "Nogo-A at CNS paranodes is a ligand of Caspr: possible regulation of K(+) channel localization". The EMBO Journal. 22 (21): 5666–78. doi:10.1093/emboj/cdg570. PMC 275427. PMID 14592966.

This article incorporates text from the United States National Library of Medicine, which is in the public domain.